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Neurology
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March 1, 1993
Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)
R C Griggs, R T Moxley, J R Mendell, et al.
Annals of Neurology
|
October 1, 1986
Subacute sensory neuronopathy secondary to dorsal root ganglionitis in primary Sjögren's syndrome
K Malinow, G D Yannakakis, S M Glusman, et al.
Neurology
|
July 28, 2004
Polymyositis: an overdiagnosed entity
F W Miller, L G Rider, P H Plotz, et al.
Neurology
|
April 26, 2001
A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy
G M Fenichel, R C Griggs, J Kissel, et al.
Annals of Neurology
|
June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients
F M Santorelli, M Sciacco, K Tanji, et al.
Neurology
|
March 31, 2012
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy
M B Harms, K M Ori-McKenney, M Scoto, et al.
Molecular Genetics and Metabolism
|
December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
M J Kovach, B Waggoner, S M Leal, et al.
Neurology
|
August 5, 2011
Phase II screening trial of lithium carbonate in amyotrophic lateral sclerosis: examining a more efficient trial design
R G Miller, D H Moore, D A Forshew, et al.
Neurology
|
July 15, 2011
Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy
D M Escolar, L P Hache, P R Clemens, et al.
Neurology
|
December 14, 2005
Tolerance of high-dose (3,000 mg/day) coenzyme Q10 in ALS
K L Ferrante, J Shefner, H Zhang, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 151) with videos related to
Sort By:
Page
of 16
Neurology
|
March 1, 1993
Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)
R C Griggs, R T Moxley, J R Mendell, et al.
Annals of Neurology
|
October 1, 1986
Subacute sensory neuronopathy secondary to dorsal root ganglionitis in primary Sjögren's syndrome
K Malinow, G D Yannakakis, S M Glusman, et al.
Neurology
|
July 28, 2004
Polymyositis: an overdiagnosed entity
F W Miller, L G Rider, P H Plotz, et al.
Neurology
|
April 26, 2001
A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy
G M Fenichel, R C Griggs, J Kissel, et al.
Annals of Neurology
|
June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients
F M Santorelli, M Sciacco, K Tanji, et al.
Neurology
|
March 31, 2012
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy
M B Harms, K M Ori-McKenney, M Scoto, et al.
Molecular Genetics and Metabolism
|
December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
M J Kovach, B Waggoner, S M Leal, et al.
Neurology
|
August 5, 2011
Phase II screening trial of lithium carbonate in amyotrophic lateral sclerosis: examining a more efficient trial design
R G Miller, D H Moore, D A Forshew, et al.
Neurology
|
July 15, 2011
Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy
D M Escolar, L P Hache, P R Clemens, et al.
Neurology
|
December 14, 2005
Tolerance of high-dose (3,000 mg/day) coenzyme Q10 in ALS
K L Ferrante, J Shefner, H Zhang, et al.
Page
of 16